Filla A - Search Results

1

Two novel CYP7B1 mutations in Italian families with SPG5: a clinical and genetic study.

Criscuolo C, Filla A, Coppola G, Rinaldi C, Carbone R, Pinto S, Wang Q, de Leva MF, Salvatore E, Banfi S, Brunetti A, Quarantelli M, Geschwind DH, Pappatà S, De Michele G. Criscuolo C, et al. Among authors: filla a. J Neurol. 2009 Aug;256(8):1252-7. doi: 10.1007/s00415-009-5109-3. Epub 2009 Apr 12. J Neurol. 2009. PMID: 19363635

2

Smell and taste acuity in epileptic syndromes.

Campanella G, Filla A, De Michele G. Campanella G, et al. Among authors: filla a. Eur Neurol. 1978;17(3):136-41. doi: 10.1159/000114936. Eur Neurol. 1978. PMID: 658058

3

Classifications of hereditary ataxias. A critical overview.

Campanella G, Filla A, De Michele G. Campanella G, et al. Among authors: filla a. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):408-19. Acta Neurol (Napoli). 1992. PMID: 1293984 Review.

4

Early onset hereditary ataxias of unknown etiology. Review of a personal series.

Filla A, De Michele G, Barbieri F, Campanella G. Filla A, et al. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):420-30. Acta Neurol (Napoli). 1992. PMID: 1293985 Review.

5

Friedreich's disease. A linkage study in southern and central Italy.

Cavalcanti F, Cocozza S, Filla A, De Michele G, Pianese L, Porcellini A, Monticelli A, Pandolfo M, Banfi S, Varrone S, et al. Cavalcanti F, et al. Among authors: filla a. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):519-23. Acta Neurol (Napoli). 1992. PMID: 1363458

6

Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of Italy.

Filla A, De Michele G, Marconi R, Bucci L, Carillo C, Castellano AE, Iorio L, Kniahynicki C, Rossi F, Campanella G. Filla A, et al. J Neurol. 1992 Jul;239(6):351-3. doi: 10.1007/BF00867594. J Neurol. 1992. PMID: 1512613

7

Influence of age, gender, height and education on vibration sense. A study by tuning fork in 192 normal subjects.

De Michele G, Filla A, Coppola N, Bisogno A, Trombetta L, Santorelli F, Campanella G. De Michele G, et al. Among authors: filla a. J Neurol Sci. 1991 Oct;105(2):155-8. doi: 10.1016/0022-510x(91)90139-x. J Neurol Sci. 1991. PMID: 1757791

8

Intrafamilial phenotype variation in Friedreich's disease: possible exceptions to diagnostic criteria.

Filla A, De Michele G, Cavalcanti F, Santorelli F, Santoro L, Campanella G. Filla A, et al. J Neurol. 1991 Jun;238(3):147-50. doi: 10.1007/BF00319681. J Neurol. 1991. PMID: 1869890

9

Cerebellar ataxia and hypogonadism. A clinicopathological report.

De Michele G, Filla A, D'Armiento FP, Striano S, Barbieri F, Salvatore G, Di Carlo V, Mansi D. De Michele G, et al. Among authors: filla a. Clin Neurol Neurosurg. 1990;92(1):67-70. doi: 10.1016/0303-8467(90)90010-3. Clin Neurol Neurosurg. 1990. PMID: 2154358

10

Clinical and genetic heterogeneity in early onset cerebellar ataxia with retained tendon reflexes.

Filla A, De Michele G, Cavalcanti F, Perretti A, Santoro L, Barbieri F, D'Arienzo G, Campanella G. Filla A, et al. J Neurol Neurosurg Psychiatry. 1990 Aug;53(8):667-70. doi: 10.1136/jnnp.53.8.667. J Neurol Neurosurg Psychiatry. 1990. PMID: 2213043 Free PMC article.

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